Junior Clinical Research Coordinator: Start-Up & Data

Beth Israel Lahey Health; New Jersey; On-site; USD 29,000 - 37,000; Full time

Job summary

Beth Israel Lahey Health is seeking a Research Study Coordinator to support multiple clinical trials under general supervision. The role involves implementing study protocols, coordinating start-up activities, and ensuring regulatory compliance with FDA, OHRP, and GCP standards.

You will recruit participants, obtain informed consent, manage data collection, and collaborate with investigators and departments to ensure protocol adherence and timely reporting.

Qualifications

• Bachelor’s degree required.
• 0-2+ years experience in a research or medical setting.
• Strong organizational and communication skills.
• Ability to travel nationally as required.

Responsibilities

• Coordinate different phases of research studies with varying complexity under moderate oversight.
• Implement study protocols in accordance with SOPs, FDA, OHRP and GCP regulations.
• Prepare and submit regulatory documents and IRB materials in a timely manner.
• Manage study start-up activities and regulatory compliance across departments.
• Recruit and screen study participants; obtain informed consent where applicable.
• Monitor data quality and ensure proper documentation in EMR and CRF systems.
• Maintain study supplies and liaise with sponsors/CROs during monitoring and audits.

Skills

Organizational skills

Multi-tasking

Attention to detail

Communication skills

Independent work

Teamwork

Education

Bachelor's degree

Job description

Beth Israel Lahey Health is seeking a Research Study Coordinator to support multiple clinical trials under general supervision. The role involves implementing study protocols, coordinating start-up activities, and ensuring regulatory compliance with FDA, OHRP, and GCP standards.

You will recruit participants, obtain informed consent, manage data collection, and collaborate with investigators and departments to ensure protocol adherence and timely reporting.